862785-22-6

Basic information

• Product Name: 2-methoxy-4-[1-(3,4,5-trimethoxyphenyl)-meth-(Z)-ylidene]-dihydrofuran-3,3-dicarboxylic acid dimethyl ester
• Synonyms: 2-methoxy-4-[1-(3,4,5-trimethoxyphenyl)-meth-(Z)-ylidene]-dihydrofuran-3,3-dicarboxylic acid dimethyl ester
• CAS NO: 862785-22-6
• Molecular Weight: 396.394
• Mol File: 862785-22-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-methoxy-4-[1-(3,4,5-trimethoxyphenyl)-meth-(Z)-ylidene]-dihydrofuran-3,3-dicarboxylic acid dimethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methoxy-4-[1-(3,4,5-trimethoxyphenyl)-meth-(Z)-ylidene]-dihydrofuran-3,3-dicarboxylic acid dimethyl ester(862785-22-6)
• EPA Substance Registry System: 2-methoxy-4-[1-(3,4,5-trimethoxyphenyl)-meth-(Z)-ylidene]-dihydrofuran-3,3-dicarboxylic acid dimethyl ester(862785-22-6)

Safety Data

• Hazardous Substances Data: 862785-22-6(Hazardous Substances Data)

Upstream product

• 25245-29-8 5-iodo-1,2,3-trimethoxybenzene 
• 22398-14-7 dimethyl (methoxymethylene)malonate 
• 107-19-7 propargyl alcohol 

Downstream Products

• 101751-72-8 trans-α-(3,4-methylenedioxybenzyl)-β-(3,4,5-trimethoxybenzyl)-γ-butyrolactone 
• 101751-72-8 cis-α-(3,4-methylenedioxybenzyl)-β-(3,4,5-trimethoxybenzyl)-γ-butyrolactone 

Relevant articles and documents

Selective Lewis acid catalyzed transformation (γ-butyrolactone versus cyclopropane) of 2-methoxy-4-benzyltetrahydrofuran derivatives. Efficient synthesis of lignan lactones

(Chemical Equation Presented) A short synthesis of lactone lignans exploiting a three-component coupling strategy is presented using a new Lewis acid catalyzed ring-opening/cyclization reaction of 2-methoxytetrahydrofuran derivatives 4 leading to γ-butyro